BostonFull TimeHuman Resources
Remotely
regulatory compliancedatachromatographygmphplcuplclnpgood documentation practices
Job Description
📋 Description
- Review analytical data packages from stability studies, method development, and investigations for
- Evaluate OOS/OOT investigation reports for completeness and scientific soundness.
- Verify calculations, data transcriptions, and chromatographic data for accuracy and regulatory
- Ensure documentation adheres to GMP and applicable regulatory guidelines.
- Maintain review timelines and tracking logs to support release and regulatory submission deadlines.
- Partner with analytical and quality teams to resolve data discrepancies and review findings.
🎯 Requirements
- B.S. in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field with 3-4 years of GMP
- Proficiency in GMP regulations and Good Documentation Practices.
- Understanding of chromatography operation and data interpretation.
- Strong organizational, time management, and cross-functional collaboration skills.
- Effective communication and documentation skills.
🎁 Benefits
- Excellent full-time benefits including medical, dental, vision, life and disability insurance.
- 401(k) with company match, paid vacation and holidays.
- Salary range: $36.00-$40.00 per hour, dependent on education/experience.
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